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Article

Factors V Leiden and the prothrombin gene mutation: two common genetic defects associated with thrombosis.

The Western journal of medicine - 1 Jun 1998

Kujovich J L, Goodnight S H

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 9655996
PMCID: PMC1305072

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Factors V Leiden and the prothrombin gene mutation: two common genetic defects associated with thrombosis.PMID 9655996Read ↗

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Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.Semantic proximity Read ↗

Association of factor V Leiden and prothrombin gene mutation with Behçet's disease.Semantic proximity Read ↗

Prothrombin and the prothrombin 20210 G to A polymorphism: their relationship with hypercoagulability and thrombosis.Semantic proximity Read ↗

A mutation in the prothrombin gene contributing to venous thrombosis during pregnancy.Semantic proximity Read ↗

Thrombosis in a patient with combined homozygosity for the factor V Leiden mutation and a mutation in the 3'-untranslated region of the prothrombin gene.Semantic proximity Read ↗

Prothrombin G20210A Polymorphism and ThrombophiliaSemantic proximity Read ↗

Venous thromboembolism in a young woman with combined homozygosity for factor V Leiden and prothrombin G20210A mutations.Semantic proximity Read ↗

Arterial and venous thrombosis and prothrombotic fibrin clot phenotype in a Polish family with type 1 antithrombin deficiency (antithrombin Krakow).Semantic proximity Read ↗

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